MXPA97010504A - Compositions detergents liquid, non-aqueous, containing particles, that include a surgical agent of alquilbencensulfon - Google Patents

Compositions detergents liquid, non-aqueous, containing particles, that include a surgical agent of alquilbencensulfon

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Publication number
MXPA97010504A
MXPA97010504A MXPA/A/1997/010504A MX9710504A MXPA97010504A MX PA97010504 A MXPA97010504 A MX PA97010504A MX 9710504 A MX9710504 A MX 9710504A MX PA97010504 A MXPA97010504 A MX PA97010504A
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Mexico
Prior art keywords
composition
weight
aqueous
liquid
acid
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Application number
MXPA/A/1997/010504A
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Spanish (es)
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MX9710504A (en
Inventor
De Buzzaccarini Francesco
Allen Smerznak Mark
John Becks Vincent
Original Assignee
John Becks Vincent
De Buzzaccarini Francesco
Allen Smerznak Mark
The Procter & Gamble Company
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Priority claimed from PCT/US1996/007814 external-priority patent/WO1997000938A1/en
Application filed by John Becks Vincent, De Buzzaccarini Francesco, Allen Smerznak Mark, The Procter & Gamble Company filed Critical John Becks Vincent
Publication of MX9710504A publication Critical patent/MX9710504A/en
Publication of MXPA97010504A publication Critical patent/MXPA97010504A/en

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Abstract

Liquid, non-aqueous and particulate containing laundry detergent compositions are described which are in the form of a suspension of particulate material, preferably including a peroxygen bleaching agent and an organic builder, dispersed in a liquid phase containing a alkylbenzene sulfonate anionic surfactant, a nonionic ethoxylated alcohol surfactant and a non-aqueous, low polarity organic solvent, said compositions provide a cleaning and bleaching of fabrics which are washed with them especially desirable and also exhibit a drawability and Especially desirable phase and chemical stability

Description

COMPOSITIONS NON-AQUEOUS LIQUID DETERGENTS, CONTAINING PARTICLES THAT INCLUDE A SURFACTANT OF ALKYLBENCENSULPHONATE FIELD OF THE INVENTION This invention relates to liquid laundry detergent products which are non-aqueous in nature and which are in the form of stable dispersions of particulate material such as blantjueo agents and / or other auxiliaries of the detergent composition. tea.
BACKGROUND OF THE INVENTION Commonly, the use of liquid detergent products is considered more convenient than particulate or powder detergent products. Therefore, liquid detergents have long been used by consumers. Said liquid detergent products are easily measurable, quickly dissolve in the wash water, are capable of being easily applied in concentrated solutions or dispersions to soiled areas on garments that will be washed and do not create dust. They also normally occupy less storage space than granulated products. Additionally, liquefied detergents may have incorporated in their formulations materials that could not support the drying operations without deterioration, operations that are commonly used in the manufacture of detergent products in particles or g nullified- *. Although liquid detergents have a number < The advantages over granular detergent products also have several disadvantages. In particular *, the components of the detergent composition which may be compatible with each other in the granulated products may tend to interact or react with each other in a liquid environment and especially an aqueous liquid environment. In this way, components such as enzymes, surfactants, perfumes, brighteners, solvents and especially bleaches and activators and bleaching can be * especially difficult to incorporate * in liquid detergent products that have a degree of esti-1. 1ad acceptable chemistry. One approach to increasing the chemical compatibility of the components of the detergent composition in liquid detergent products has been that of formulating liquid non-aqueous (or anhydrous) detergent compositions. In said non-aqueous products, at least a part of the components of the solid detergent composition normally tend to remain soluble in the liquid product and are therefore less reactive with each other, than if they had been released in the liquid matrix. . Non-aqueous liquid detergent compositions, including those containing reactive materials such as peroxy ono bleaching agents. they have been described for example in, Hepworth et al., U.S. No. 4,615,820, issued October 17, 1986; Chultz et al., patent of F.U.A. No. 4,929,380, issued May 29, 1990; Schultz and others, patent of E.U.A. No. 5,008,031, issued April 16, 1991; Eider * et al., EP-A-030,096, published on August 10, 1901; Hall et al., UO 92/09670, published June 11, 1992 and Sandersson et al., EP-A-565, 017, published October 13, 1993. Although the chemical compatibility of the components can be increased in the liquid non-aqueous detergent compositions, the physical stability of said compositions can become a problem. This is because there is a tendency for such products to separate in phases as drops of solid insoluble particles dispersed from the suspension and settle to the bottom of the container containing the liquid detergent product. As a consequence of this type of problem, there may also be difficulties associated with incorporating sufficient types and adequate amounts of surfactant materials into non-aqueous liquid detergent products. The surfactant materials must, of course, be selected to be suitable for imparting an acceptable fabric cleaning performance to said compositions., but the use of such materials should not lead to an unacceptable degree of phase separation of the composition. Phase stabilizers, such as thickeners or viscosity control agents, should be added to these products to improve the physical properties of the same. However, said materials can add cost and bulk to the product without contributing to the washing / cleaning performance of said detergent compositions. It is also possible to select surfactant systems for said liquid laundry detergent products that can actually impart a structure to the liquid phase of the product and thus promote the suspension of the particulate components disposed within said structured liquid phase. An example of such a product with a structured surfactant system is found in van der Hoeven and others; patent of E.U.A. No. 5,389,284, issued February 14, 1995, which uses a system of surfactant surfactant based on relatively high concentrations of nonionic surfactants of aleoxi alcohol and ammonium deflocculating agents. In products employing a structured surfactant system, the liquid phase must be sufficiently viscous to prevent sedimentation and phase separation of the suspended particulate material, but not so viscous that the Emptying and dispensability of the detergent product will be adversely affected. According to the above, there is clearly a continuing need to identify and provide detergent compositions containing particles and liquids in the form of non-aqueous liquid products having a high degree of chemical stability, e.g., blantjueador and enzyme, together with a stability of commercial phase AoeptabLe, emptying capacity and performance of blan «cleaning, cleaning or washing of the composition 5 detergent. Accordingly, it is an object of the present invention to provide liquid detergent products which contain particulate and non-aqueous detergents which have such particularly desirable characteristics of chemical and physical stability, as well as a surprising pouring capacity and characteristics of LU washing and bleaching performance. of fabrics.
BRIEF DESCRIPTION OF THE INVENTION The present invention provides non-aqueous liquid detergent compositions comprising a stable suspension of solid, soluable, solid particulate material dispersed through a liquid phase containing surfactant and structured agent. Said compositions comprise A) of about 35% to 99% by weight of the 2U composition of a non-aqueous liquid phase; and B) from about 1% to 65% by weight of the composition of one or more types of particulate materials. The non-aqueous liquid phase itself comprises from about 30% to 65% by weight of this liquid phase of a certain type of dissolved ammonium surfactant. This ammonium surfactant component comprises a material selected from the alkali metal salts of the cyclobenzene fonols of Cio-Ciß. In addition to the component of the ammonium surfactant component, the non-aqueous liquid phase of the composition of the present it also comprises from about 35% to 70% by weight of the liquid phase of a non-aqueous liquid diluent. Said diluent comprises both i) alcohol alkoxylates of the formula R1 (0CmH2m) n OH wherein R1 is an alkyl group of Cs-Cie, rn is from 2 to 4 and n is from about 2 to 1; like 11) an organic solvent of low polarity and non-aqueous. These components are present in the non-aqueous liquid diluent at a weight ratio of alkoxylated alcohol to organic solvent of from about 50: 1 to 1:50. The particulate material suspended in the nonaqueous liquid phase of the compositions herein ranges in size from about 0.1 to 1500 microns and is substantially more soluble in the non-aqueous compositions of the present invention. This insoluble particulate material comprises a blernenfe peroxygen bleach, but may also comprise bleach activators, auxiliary ammonium surfactants, organic builders, inorganic alkalinity sources and combinations of these types of particulate material. 1).: * ', DETAILED JPCL0N OF THE INVENTION The non-aqueous liquid detergent compositions of this invention comprise a surfactant and a liquid phase which contains a polarity solvent which has dispersed in the system as a solid phase certain types of particulate materials. The essential and optional components of the liquid and solid phases of the detergent compositions herein, as well as the form, preparation and use of the composition, are described in greater detail as follows: (all concentrations and relationships are on a base of weight unless otherwise specified).
LIQUID PHASE The liquid phase will generally comprise from about 35% to 99% by weight of the detergent compositions herein. Most preferably, the liquid phase will comprise from about 50% to 95% by weight of the compositions. More preferably, the liquid phase will comprise from about 45% to 75% by weight of the compositions herein. The liquid phase of the detergent compositions herein contains essentially relatively high concentrations of a certain type of ammonium surfactant combined with a certain type of liquid and non-aqueous diluent.
(A) Essential ammonium ionic agent The ionic surfactant agent used essentially as an essential component of the non-aqueous liquid phase is one selected from the alkali metal salts of alkyl-centric acids in which the alkyl group contains of approximately 10 to 16 atoms of carbon, in straight chain configuration or "branched chain". (See U.S. Patent Nos. 2,220,099 and 2,477,383, incorporated herein by way of reference). Sodium and potassium linear straight chain alkyl benzene sulphonates (LAS) in which the average number of carbon atoms in the alkyl group is from about 11 to 14 are especially preferred. LAS <is especially preferred.1e sodium of On-Ci *. The alkylbenzene fonate ammonium surfactant will be dissolved in the non-aqueous diluent, which is the second essential component of the non-aqueous phase. To form * the structured liquid phase required for adequate phase stability and acceptable rheology, the alkylbenzene ammonium surfactant agent is generally present to the extent of from about 30% to 65% by weight of the liquid phase. Most preferably, the ammonium surfactant "alkylbenzene fonate" comprises from about 35% to 50% by weight of the nonaqueous liquid phase of the compositions herein. The use of this ammonium surfactant agent at these concentrations corresponds to a concentration of ammonium surfactant in the total composition from about 15% to 60% by weight, most preferably from about 20% to 40% by weight of the composition.
(B) Nonaqueous Liquid Diluent To form the liquefied phase of the detergent compositions, the alkylbenzene sulfate ammonium surfactant described hereinabove is combined with a non-aqueous liquid diluent containing two essential components. These two components are a liquid alkoxylated alcohol material and an organic solvent of low polarity and non-aqueous. i) Alcohol alkoxylates An essential component of the liquid diluent used to form * the compositions herein comprises an alkoxylated fatty alcohol material. Said materials are themselves nonionic surfactants as well. Said materials correspond to the general formula: Rl (Cm Hm 0) n OH where R 1 is an alkyl group of Cs-Cis, m is from 2 to 4 and n is from about 2 to 12. Preferably R is an alkyl group, which may be primary or secondary, containing from about 9 to 15 carbon atoms, most preferably from about 10 to 14 carbon atoms. Preferably, also the alkoxy fatty alcohols will be ethoxylated materials containing from about 2 to 12 portions of ethylene oxide per molecule, and preferably from about 3 to 10 portions of ethyl oxide per molecule. The alkoxylated fatty alcohol component of the liquid diluent will often have a hydrophobic balance (LHB) ranging from about 3 to 17. Most preferably, the HLB of this material will vary from about 15 to 15%. Examples of fatty alcohol alkoxylates useful as one of the essential components of the non-aqueous liquid diluent in the compositions herein, include those which are made from alcohols of 12 to L5 atoms. of carbon and containing approximately 7 moles of ethylene oxide. Such materials have been marketed under the trademarks Neodol 25-7 and Neodol 23-6.5 by Shell Chemical Company. Other useful Neodols include Neodol 1-5, a fatty alcohol ethoxylated that averages 11 carbon atoms in its alkyl chain with about 5 moles of ethylene oxide; Neodol 23-9, a C12-C13 primary ethoxylated alcohol having about 9 moles of ethylene oxide and Neodol 91-10, a C9-C11 primary ethoxylated alcohol having approximately 10 moles of ethylene oxide. Ethoxylated alcohol liquors of this type have also been marketed by Shell Chemical Company under the Dobanol brand. Dobanol 91-5 is an ethoxylated C9-C11 fatty alcohol with an average of 5 moles of 1 J oxide of Oxygen and Dobanol 25-7 is a fatty alcohol et of Ci2 ~ 0i5 with an average of 7 moles of ethylene oxide per mole of fatty alcohol. Other examples of suitable ethoxy side alcohols include Tergitol L5-S-7 and Tergitol 15-S-9, both of which are ethoxy sides of linear secondary alcohol which have been commercialized by * Union Carbide Corporation. The first is a mixed ethoxylation product of a secondary linear alkanol from Cu to Cis with 7 moles of ethylene oxide and the latter is a similar product * but with 9 moles of full-oxide reacted. Other types of alcohol ethoxylates useful in the present compositions are the higher molecular weight nonionics, such as Neodol 45-11, which are similar condensation products of ethylene oxide of higher fatty alcohols, with the highest fatty alcohol being of 14-15 carbon atoms and the number of oxide and ethylene groups per mole being approximately 11. These products have also been marketed by Shell Chemical Cornpany. The alcohol component which is essentially used as part of the liquid diluent in the non-aqueous compositions will be present generally to the extent of about 1% to 60% of the liquid phase composition. Most preferably, the alkoxylated alcohol component will comprise from about 5% to 40% of the liquid phase. More preferably, the alcohol alkoxylation component used will essentially comprise from about 5% to 30% of the liquid phase of the detergent composition. The use of alcohol in these concentrations in phase 1 corresponds to an alkoxylated alcohol concentration in the total composition from about 1% to 60% by weight, very preferably from about 2% to 40% by weight, and more preferably from about 5% to 25% by weight of the composition. ii) Organic Polarity and Non-Aqueous Organic Solvent A second essential component of the liquid diluent that forms part of the liquid phase of the detergent compositions herein, comprises low polarity and non-aqueous organogist (s) ( s). The term "solvent" is used herein to refer to the diluent or non-active carrier portion on the surface of the liquid phase of the composition. Although some of the essential and / or optional components of the compositions herein may come to dissolve in the liquid phase containing "solvent", other components will be present as particulate material dispersed within the liquid phase containing "solvent" . In this way, the term "solvent" is not designed to require that the solvent material be capable of actually dissolving all of the components of the detergent composition added thereto. The non-aqueous organic materials that are used herein are those that are polarity-free liquids For the purposes of this invention, "low-polarity" liquids are those that have very little if they have , tendency to dissolve one of the preferred types of particulate material used in the compositions herein, and say *, the peroxygen bleach, sodium per-borate or sodium percarbonate agents. relatively polar solvents such as ethanol Suitable types of low polarity solvents useful in the liquid and non-aqueous detergent compositions herein include non-vicinal C4-C8 alkylene glycols, mono-lower alkylene glycol alkyl ethers, weight polyethylene glycols lower molecular weight, lower molecular weight methyl esters and amides, and the like A preferred type of non-aqueous low polarity solvent for use in composites The present invention comprises the non-vicinal straight or branched chain glycols of the C4-C8 chain. Materials of this type include hexylene glycol, (4-rnet? L -2, 4-pentanodol), 1,6-hexanodol, 1,3-butylene glycol and 1,4-butylene glycol. Illeglycol hex is the most preferred. Another preferred type of polarity and non-aqueous solvent that is used herein comprises the C2-C6 monoalkyl esters of mono-, di-, tri- or tetra-alkylene glycol of C2-C3. Specific examples of such compounds include monobutyl ether of diet i longl icol, oter onobut? L? coe tet raet ilengl icol, ether rnonoet i Li co of diprop lengL LCOI and ether * monobutyl of di propylene glycol. Especially preferred are the rnononobutyl LCO ether of dLetilengl col and the nonobutyl ether of dipropylene glycol. The compounds of this type have been marketed under the trademarks Do anol, Carbitol, and Cellosol ve. Another preferred type of organic solvent of low polarity and non-aqueous useful herein comprises the polyethylene glycols of low molecular weight (PEGs). Said materials are those that have molecular weights of at least about 150. PEGs of molecular weight ranging from about 200 to 600 are the most preferred. Also another preferred type of non-aqueous and non-polar solvent comprises the low molecular weight methyl esters. Said materials are those of the general formula: R -C (0) -0CH3 wherein R1 ranges from 1 to 18. Examples of suitable low molecular weight methyl esters include methyl ether, methyl propionate, methyl octanoate and dodecanoate of methyl. The organic solvent (s) of low polarity and non-aqueous employed must, of course, be compatible and non-reactive with other components of the composition, eg, bleach and / or activators, used in the liquid detergent compositions of the prior art. nte. Said solvent component will generally be used in an amount of from about L% to 70% by weight of the Lujuuia phase. Preferably, the low and non-aqueous organic solvent will suitably comprise 10% to 60% by weight of the liquid phase., more preferably from about 20% to 50% by weight, of the liquid phase of the composition. The use of this organic solvent at these concentrations in the liquid phase corresponds to solvent concentration in the total composition of from about 1% to 50% by weight, most preferably from about 5% to 40% by weight, and more preferably about 10% to 30% by weight of the co-position. iii) Alkoxylation ratio of alcohol to solvent The ratio of alcohol alkoxylation to organic solvent within the liquid diluent can be used * to vary the rheological properties of the detergent compositions eventually formed. Generally, the weight ratio of the alkoxylate of alcohol to the organic solvent will vary from about 50: 1 to 1:50. Most preferably, this ratio will vary from about 3: 1 to 1: 3. iv Concentration of the liquid diluent Like the concentration of the alkylbenzene sulfonate ammonium surfactant mixture, the amount of total liquid diluent in the nonaqueous liquid phase of the present will be determined by the type and amounts of other Ib components of the composition and by the composition of the composition "leseadas. Generally, the lujuid diluent will comprise from about 35% to 70% of the non-aqueous liquid phase of the compositions herein. Most preferably, the liquid diluent will comprise from about 50% to 65% of the non-aqueous liquefied phase. This corresponds to a concentration of non-aqueous liquid diluent in the total composition of from about 15% to 70% by weight, preferably about 20% to 50% by weight, of the composition.
SOLID PHASE The non-aqueous detergent compositions herein also essentially comprise from about 1% to 65% by weight, most preferably from 5% to 50% by weight, of a solid phase of particulate material which is dispersed and suspended within the liquid phase. . Generally said particulate material will vary in volume from about 0.1 to 1500 microns. Most preferably, said material will vary in size from about 5 to 200 microns. The particulate material used herein may comprise one or more types of detergent composition components which, in particulate form, are substantially soluble in the nonaqueous liquid phase of the composition. The types of particulate materials that can be used are described in "Jet alie as follows: (A) Peroxygen bleaching agent with optional bleach activators The most preferred type of particulate material useful for fopnar The solid phase of the detergent compositions herein comprises particles of a peroxygen bleach agent. Said peroxygen bleaching agents may be organic or inorganic in nature. Inorganic peroxygen bleaching agents are often used in combination with a bleach activator. Suitable organic peroxygen bleaching agents include percarboxylic acid bleaching agents and salts thereof. Suitable examples of this class of agents include magnesium monoperoxy t alato hexahydrate, magnesium salt of rnetachlor perbenzoic acid, 4-non? Larmno-4-oxoperox acid? buty ico and acid diperox i dodecanodioi co. Said bLanqueo agents are described in the patent of E.U.A. No. 4,483,781, Hrtrnan, issued on November 20, 1984; in European patent application EP-A-133,354, Banks et al., published February 20, 1985; and in the patent of E.U.A. No. 4,412,934 Chung et al., Issued November 1, 1983. Highly preferred bleaching agents also include 6-non? Lam acid. no-6-oxoperoxycaproic acid (NAPAA) such as that described in the US patent. No. 4,634,551, issued on January 6, 1987 to Burns y tro. The inorganic peroxy bleach agents can also be used in the form of particles in the present "Jetting" compositions. In fact, inorganic bleaching agents are preferred. Such inorganic peroxygen compounds include percarbonate and perborate materials, alkali metal, and preferably percarbonates. For example, sodium perborate (e.g., mono-or tet rahí dratado) can be used. Suitable inorganic bleaching agents may also include * sodium or potassium carbonate peroxyhydrate and equivalent "percarbonate" bleaches, peroxide peroxide hydrated sodium pyro, drained peroxyhi urea, and sodium peroxide. Persulfate bleach (e.g., OXONE manufactured commercially by DuPont) can also be used. Frequently, the inorganic peroxygen bleaches will be coated with silicate, borate, sulfate or water-soluble surfactants. For example, the coated percarbonate particles are available from various commercial sources such as FMC, Solvay, Interox, Tokai Den a and Degussa. Inorganic peroxygen bleaching agents, e.g., perborates, percarbonates, etc., are preferably combined with bleach activators that lead to in situ production in the aqueous solution (i.e., during the use of the compositions of the present for the washing / bleaching of fabrics) of the peroxy acid corresponding to the bleach activator. Several non-limiting examples of activators are described in the U.S. patent. No. 4,915,854, issued April 10, 1990 to Mao et al., And in U.S. Patent No. 4,412,934, issued November 1, 1983 to Chung et al. Activators of nonanoyloxybenzenesulfonat? (NOTIC) and tetraacetic tetraacetate (TAED) are typical. You can also use * them rnezcLas of them. See also the patent of E.U.A. No. 4,634,551 previously mentioned, for other blanks, and typical activators and useful in the present. Other activators of nest-depurated bleaching are those of the formulas: Rl N (R5) C (O) R2 C (0) LO Rl C (0) N (RS) R2 C (O) L where Rl is an alkyl group which contains from 6 to about 12 carbon atoms, R2 is an alkylene containing from about 1 to about 6 carbon atoms, R5 is H or alkyl, aryl, or alloy which contains approximately 1 to about 10 carbon atoms, and L is any suitable starting group. A starting group is any group that is displaced from the bleach activator * as a consequence of the nucleophilic attack on the bleach activator by the peri drolysis anion. A preferred starting group is the phenol sulfonate. Preferred examples of bleach activators of the above formulas include (6-oc + anam? O-caproyl) or? benzenesulonate, (6-nonanarn? doca? ro?) oxybenzenesulfonate, (6-decanarnide-caproyl) oxobenzenesulfonate and mixtures thereof as described in the patent of F..U.A. Do not. 4,634,551 mentioned above. Said mixtures are characterized in the present case (6 - al cami do-cap roí L) ox? benzenensu f onat or Cs -Cio - Another class of useful bleach activators comprise the benzoxazm activators described by Hodge et al., in the patent E.U.A. No. 4,966,723, issued October 30, 1990, incorporated herein by reference. A highly preferred activator «1 type benzoxazm is: fl / pU) Still another class of useful whitening activators includes acyl lactase activators, especially the acyl caprolactans and aci 1 valerolactains of the formulas: f2 / pl0 wherein 6 is H or an alkyl, aryl, alkoxyaryl or alean group containing from 1 to about 12 carbon atoms. Activators include highly prefendos lactam caprolactarna benzol 1, octanoyl caprolactarna, 3,5,5-t prneti 1 1 caprolactarna hexanol, nonanoyl caprolactam, caprolactam decane l, capr undeconoil * olactama, benzoyl valerolactam, octanoyl valerolactarna, valerolactarna decanoyl, und cenoi 1 valerolactarna, 3, 5, -tprnet? ihexano? l valerol actarria and mixtures thereof. See also the patent of E.U.A. No. 4,545,784, issued to Sanderson on October 8, 1985, incorporated herein by reference, which discloses acyl caprolactams, including benzoyl caprolactane, adsorbed on sodium perborate. If peroxygen bleaching agents are used as all or part of the particulate material essentially present, they will generally comprise from about 1% to 30% by weight of the composition. Most preferably, the peroxygen bleaching agent comprises from about 1% to 20% by weight of the composition. More preferably, the peroxygen bleaching agent will be present to the extent of from about 3% to 15% by weight of the composition. If used, the bleach activators can comprise from about 0.5% to 20%, preferably, from about 1% to 10% by weight of the composition. Frequently, activators are used so that the molar ratio of bleaching agent to activator ranges from about 1: 1 to 10: 1, preferably, about 1.5: 1 to 5: 1. In addition, it has been discovered that bleaching actives, when agglomerated with certain acids such as CL acid, are more stable than metal.
Ib) tensioactivoß auxiliary agents aniónicoß Another possible type of particulate material which can be suspended in the nonaqueous liquid detergent compositions herein includes ancillary agents ivos tensioact ammonium "? Ue are fully or partially insoluble in the nonaqueous phase lLquida. The most common type of ammonium surfactant with said solubility properties comprises the primary or secondary alkylsulfate ammonium surfactants. These surfactants are those produced by the sulfation of higher fatty alcohols Je C8-C20. Surfactants conventional primary alkyl have the general formula: R0S03-M + don 'Je R is typically a Lo linear hidrocarbí group of Ce-C20 alkyl which may be straight chain and branched chain, and M is a solubilized cation in water . Preferably, R is a C 1 or C 0 alkyl and M is alkaline metal. Most preferably, R is approximately C12 and M is sodium. The conventional secondary alkyl sulfates can also be used as the essential ammonium surfactant component of the solid phase of the compositions herein. Conventional secondary surfactants and surfactants are those materials that have the sulphate portion di st pbuted through the "hydrocarbon base structure" Lo of the molecule. Such materials can be illustrated by the structure: CH3 (CH2) n (CH0S03-M +) (CH2) mCH3 where in and n are integers of 2 or more, and the sum of m + n is typically from about 9 to 15, and M is a soluble cation soluble in water. If all or part of the necessary particulate material is used, auxiliary ammonia agents such as alkylsulphates will co-generate approximately 1% to 10% by weight of the composition, preferably from about 1% by weight. % to 5% by weight of the composition. The alkyl sulfate used as all or part of the particulate material is prepared and added to the compositions herein separately from the non-alkoxylated alkyl sulphate material which may be part of the alkyl ether sulfate surfactant component essentially used as part of the the liquid phase of the present.
(C) Organic builder material Another possible type of particulate material that can be * suspended in the liquid and non-aqueous detergent compositions herein comprises an organic de-inking material that counteracts the effects of calcium or other ion , The hardness of the water found during use «le 1 ava < the white of the compositions of the present. Examples of said killings for Les include alkali metal, citrates, succmates, bad onatos, fatty acids, carboxymethyl succinates, carboxylates, polycarboxylates and polylacetyl carboxylates. Speci fi c axes include sodium, potassium, and lithium salts of oxydisciac acid, melitic acid, benzenepolycarboxylic acids, and citric acid. Other examples of organic phosphonate type sequestrants such as those sold by Monsanto under the trade name Dequest and alkanohydroxy phosphonates. The salts of treatment are also highly preferable. Other suitable organic builders and detergents include the highest molecular weight polymers and copolymers known to have improving properties < 1e detergency. For example, said materials include poly acrylic acid, polymaleic acid and polyacrylic acid / polyacrylic acid copolymers and their salts, such as those sold by BASF under the trademark Sol-al n. Another suitable type of organic detergent builder comprises the water soluble salts of higher fatty acids, ie, "soaps". These include alcaline rnetal soaps such as sodium, potassium, ammonium and sodium salts.
The ammonium salt of higher fatty acids contains from about 8 to about 24 carbon atoms, and preferably from about 12 to about 18 carbon atoms. Soaps can be manufactured by direct saponification of fats and oils or medLanto The neutralization of udder fatty acids. Particularly CitiLes are the sodium and potassium salts of the fatty acid mixtures derived from coconut oil and tallow, that is, sodium and potassium tallow and coconut soap. If all or part of the necessary particulate material is used, the insoluble organophosphorous agents can generally comprise from 2% to 20% by weight of the compositions herein. Most preferably, said builder material may comprise * from about 4% to 10% by weight of the composition.
(D) Sources of inorganic alkalinity Another possible type of particulate materials that can be suspended in the non-aqueous liquid detergent compositions herein may comprise a material that serves to make aqueous wash solutions formed from said generally alkaline compositions. in nature Said materials may or may not also act as detergency builders, that is, as materials that counteract the adverse effect of water hardness on the detergency performance. Examples of suitable alkalinity sources include carbonates, bicarbonates, borates, siLicates and alkali metal inetasilicates soluble in water. Although not preferred for ecological reasons, water-soluble phosphate salts can also be used as sources of alkalinity. These include the ?? phosphates, orthophosphates, polyphosphates and alkali metal phosphonates. Of all these sources, the most preferred are alkaline metal carbonates, such as sodium carbonate. The source of alkalinity, if it is in the form of a hydratable salt, can also serve as a desiccant in the non-aqueous liquid detergent compositions herein. The presence of an alkalinity source that is also a desiccant can provide benefits in terms of chemically stabilizing those components of the composition such as the peroxygen bleach that may be susceptible to water deactivation. If it is used as all or part of the particulate component, the source of alkalinity will generally comprise from about 1% to 25% by weight of the compositions herein. Most preferably, the source of alkalinity may comprise from about 2% to 15% by weight of the composition. Such materials, although soluble in water, will generally be insoluble in the non-aqueous detergent compositions herein. In this way, said materials will generally be dispersed in the non-aqueous liquid phase in the form of "Jiscret as" particles.
OPTIONAL COMPOSITION COMPONENTS In addition to the essential components of the solid and liquid phase of the composition as described above, the compositions of the present invention can, and preferably will contain, a number of optional components. Such optional components may be in liquid or solid form. The optional components can either be dissolved in the liquid phase or they can be dispersed within the liquid phase in the form of fine particles or droplets. Some of the materials that can optionally be used in the compositions herein are described in greater detail as follows: (A) Optional surfactants Apart from the essentially used alkylbenzene sulfonate surfactant materials and the alkoxylated alcohol component of the liquid diluent, the detergent compositions herein may also contain, in addition to the optionally described alkyl sulfates described above, other types of surfactant materials. surfactant agent. Such optional surfactants should, of course, be compatible with other components of the composition and should not affect it replaces the rheology, stability or performance of the composition adversely. The optional surfactants may be ammonium, nonionic, cationic and / or amphoteric. If they are employed, Agents < Optional surfactants will generally comprise from about 1% to 20% by weight of the compositions herein, most preferably from about 5% to 10% by weight of the compositions herein. A common type of ammonium surfactant agent material which can optionally be added to the detergent compositions herein comprises the alkyl polyallylated sulfates. Sulfated sulfates, alkylpolyols are also known as alkoxylated alkylsulphates or alkylether sulfates. Said materials are acμjellos that correspond to the formula R2-0 ~ (CmH2mO) nS? 3M where R2 is a C10-C22 alkyl group, rn is 2 to 4, n is about 15 and M is a cation salt fopnador. Preferably, R 2 is a C 1 -C 18 alkyl, r 2 is 2, n is from about 1 to 10, and M is sodium, potassium, ammonium, alkylene or alkanolar. More preferably, R2 is C12-Cis, rn is 2, n is from about 1 to 6 and M is sodium. The counterions of ammonium, alkylennon and alkanolarnon are preferably avoided when the solid phase materials used in the compositions herein include a peroxygen bleach agent.
The common type of ammonium surfactant agent which can be optionally added to the detergent compositions of the present invention comprises the ammonium carboxylate type. The ammonia t Lpo carboxylate include the C 1 or C 2 alkyl alkoxycarboxylates (especially the EO ethoxycarboxylates of 1 to 5) and the C 1 or C 2 β sarcosinates, especially oleoylsarcosmate. Another common type of ammonium surfactant material that may optionally be employed comprises sulfonated ammonium surfactants such as Cß-Cis paraflsulfonates and Cs -Cis olefinsulfonates. A preferred type of optional nonionic surfactant comprises surfactants which are polymers of oxide block of ethylene (EO) -oxide of propylene (PO). The materials of this invention are well-known nonionic surfactants which have been commercialized under the trade name Pluronic. These materials are formed by adding blocks of oxide portions to the ends of the polypropylene glycol chains to adjust the active surface properties of the resulting polymer polymers. EO-PO block polymer nonionic surfactants of this type are described in greater detail in Daviessohn and Milwdsky: Synthetic Detergent, 7th Ed; Longrnan Scientific and Techmcal (1987) on pp. 34-36 and pp. 189-191, and in the patents of E.U.A. Nos. 2, 674,619 and 2,677,700. All of these publications are incorporated herein by reference. It is believed that these Pluronic-type nonionic surfactants function as effective suspending agents for the particulate material which is dispersed in the liquid phase of the detergent compositions herein. Another preferred type of optional nonionic surfactant for use in the compositions herein, comprises polyhydroxy fatty acid amide surfactants. The materials of this type of nonionic surfactant are those that conform to the formula: wherein R is an alkyl or alkenyl of C9-17, P is 1 to 6 and Z is glycityl derived from a reduced sugar or alkoxylated derivative thereof. Such materials include the N-rnetii C12-C18 glucarnides. Examples are N-rnethyl N-l-deoxyglucilic cocoarnide and N-methyl N-1-deoxy? Glucyl ilolearnide. The processes for making polyhydroxy fatty acid amides are known and can be found, for example, in U)? Lson, U.S. Pat. No. 2,965,576 and Sch. Artz, U.S. Pat. No. 2,703,798, the descriptions of which are incorporated herein by reference. The materials themselves and their preparation are also described in greater detail in Honsa, US patent. No. 5,174, 937, issued December 26, 1992, which is also incorporated herein by reference. eleven (b) Optional inorganic detergent builders The detergent compositions herein may also optionally contain one or more types of better inorganic detergent builder than those listed above, which also function as sources of alkalinity. Such optional inorganic detergent builders may include, for example, alurnosil and such as zeolites. The zeolites of the ummosilicate and its use as detergency builders are fully described in Cor ill et al., U.S. Pat. No. 4,605,509, issued on August 12, 1986, the description of which is incorporated herein by reference. The stratified crystalline silicates, such as those described in this North American patent '509 are also suitable for use in the detergent compositions herein. If used, optional inorganic builders may comprise from about 2% to 15% by weight of the compositions herein. (c) Optional Enzymes The detergent compositions herein may also contain one or more types of detergent enzymes. Said enzymes may include proteases, amylases, cellulases and lipases. Such materials are known in the art and are available commercially. They may be "ncorporate" in non-aqueous liquid detergent compositions, such as suspensions, "disks" or "pellets". Another suitable type of enzyme comprises acids in the form of enzyme suspensions in non-toxic active agents, eg. the corneral enzymes fior Novo Nordisk ba or the commercial name "SL" or the encapsulated enzymes marketed by Novo Nordisk under the trade name "LDP". Especially preferred is the use of the enzymes added to the conventional enzyme compositions in the present invention. Said pellets will vary generally in size from about 100 to 1,000 microns, very preferably from 200 to 800 microns and will be suspended throughout the non-aqueous liquid phase of the composition. It has been found that pellets in the compositions of the present invention, in comparison with other enzyme forms, exhibit an enzymatic stability which is especially desirable in terms of retention of enzymatic activity over time. Thus, compositions using enzyme pellets do not need to contain conventional enzyme stabilization as is most often used when the enzymes are incorporated in aqueous liquid detergent compositions. If employed, the enzymes will normally be incorporated into the non-aqueous liquid compositions herein at levels sufficient to provide up to about 10 mg by weight, typically from about 0.01 mg to about 5 mg of active enzyme per * gram of the composition. In other words, the nonaqueous detergent compositions herein will typically comprise from 0.001% to 5%, preferably from 0.01% to L% by weight, of a commercial enzyme preparation. Protease enzymes, for example, are normally present in such commercial preparations at levels sufficient to provide from 0.005 to 0.1 Anson units (AU) of activeness by weight of composition. (d) Optional chelating agents The detergent compositions herein may also optionally contain a chelating agent which serves to chelate metal, eg, iron and / or manganese ions within the non-aqueous detergent compositions herein. Such chelating agents thus serve to form complexes with metal impurities in the composition "otherwise to tend to deactivate the components of the composition such as the peroxygen bleach agent. Useful chelating agents may include * arninocarboxylates, phosphonates, arninophosphonates, polyunstrutionally substituted aromatic juicers, and mixtures thereof. Useful ammocarboxylates as optional chelating agents include ethylenediaminetetraacetates, N-hydroxyeti-ethylenediamineacetates, methylpotatacetates, etiien-dianthinetrapropionates, petitlenetetraate inhexacetates, diethylenetetraninpentaacetates, etiiendiateindisuccinates, and Ethanol Ldigl? c more. The alkaline metal salts of these materials are preferred. The phosphonates are also suitable for use as chelating agents in the compositions of this invention when at least low levels of total phosphorus are allowed in the detergent compositions, and include ethylene diamine (phosphonates) as DEQUEST. Preferably, these phosphonates do not contain alkyl or alkenyl groups with more than 6 carbon atoms. Preferred chelating agents include hydroxyethyldiphosphomatic acid (HEDP), diethylene glycol-acetic acid (DTPA), acid and lendiarnindisuccimic acid (EDDS) and dipicolimic acid (DPA) and salts thereof. Of course, the chelating agent can also act as a detergency builder during the use of the compositions herein for washing / bleaching fabrics. The "jugulatory" agent, if employed, may comprise from about 0.1% to 4% by weight of the compositions herein. Most preferably, the chelating agent comprises from about 0.2% to 2% by weight of the detergent compositions herein. (e) Thickeners, viscosity control agents and / or optional dispersants The detergent compositions herein may optionally also contain a poly meric material which serves as a catalyst. to improve the ability of the composition to maintain * its components of solid particles in suspension. Said materials can then act as thickening agents, of viscosity control and / or disperse. Such materials are often polynectic carboxylates, but may include other polymethylene materials such as polyvinylpyrrolidone (PVP). Polycarboxy polycarboxylate materials can be prepared by polimerizing or copolymerizing suitable unsaturated monoerynes, preferably in their acid form. Ion-unsaturated, unsaturated acids that can be cross-linked to form suitable poly-carboxylates include acrylic acid, maleic acid (or rnalene anhydride), fumaric acid, itacomco acid, aconitic acid, mesacomco acid, nitric acid and rnetilenrnalonico aculo. The presence in pol polycarboxylates of the present of non-ionic segments that do not contain carbaxyl radicals such as ether, vinyl, styrene, ethylene, etc., is adequate. , as long as said segments do not constitute more than 40% by weight of the polymer. Particularly suitable polunencos polycarboxylates can be derived * from acrylic acid. Said acrylic acid-based polymers which are useful herein are the water-soluble salts of polyacrylic acrylic acid. The average molecular weight of said polymers in the acid form preferably ranges from about 2,000 to 16.
LO, 000, very preferably from about 4,000 to 7,000 and more preferably from about 4,000 to 5,000. The water soluble salts of said polymers and aoric acid may include, for example, the alkali metal salts. Soluble polymers of that type are known materials. The use of polyacrylates of this type in detergent compositions has been described, for example, in Diehl, U.S. Pat. No. 3,108, l) b7, issued on March 7, 1967. These materials can also act as detergency builders. If used, the thickening agents, viscosity control and / or optional dispersants should be present in the compositions herein to the extent of from about 0.1% to 4% by weight. Most preferably, said materials may comprise from approximately 0.5% to 2% by weight of the detergent compositions herein.
() Optional liquid bleach activators The detergent compositions herein may also optionally comprise bleach activators which are in liquid form at room temperature and which can be added as liquids to the non-aqueous liquid phase of the liquids. detergent compositions herein. One such liquid bleach activator is acetyl citrate citrate (ATC). Other examples include glycerol tnacetate and nonanoyl valerolactam. Liquid bleach activators can be dissolved in the non-aqueous liquid phase of the compositions of the invention. the present. (g) Optional brighteners, suds suppressors, colorants and / or perfumes The detergent compositions herein may optionally also contain polishes, suds suppressors, ilicon oils, whitening catalysts, colorants and / or conventional perfume materials. Of course, said openings, foam suppressors, ilicon oils, bleach catalysts, dyes and perfumes, must be compatible and not reactive with the "components of the composition in a non-aqueous environment. If present, the brighteners, foam suppressors, colorants and / or perfumes will typically comprise from about 0.0001% to 2% by weight of the compositions herein. Suitable bleach catalysts include the manganese-based complexes described in EU 5,246,621, EU 5,244,594, EU 5,114,606 and EU 5,114,611.
FORM OF COMPOSITION As indicated, the non-aqueous liquid detergent compositions herein are in the form of bleaching agent and / or other particulate materials as a solid phase suspended in, and dispersed through, a non-aqueous liquid phase. Generally, the non-aqueous liquid phase will comprise < from about 35% to 99%, most preferably from about 50% to 95% by weight of the composition, the solid phase dispersed from about 1% to 65%, most preferably from 5% to 50% by weight weight of the composition. The liquid detergent compositions containing particles of this invention are substantially non-aqueous (or anhydrous) in character. Although very small amounts of water may be incorporated into such compositions as an impurity in the essential or optional components, the amount of water should in no case exceed approximately 5% by weight of the compositions herein. More preferably, the water content of the non-aqueous detergent compositions herein will comprise less than about 1% by weight. The non-aqueous liquid detergent compositions containing particles herein will be relatively viscous and phase stable under commercial conditions and use of said compositions. Frequently, the viscosity of the compositions herein will vary from about 300 to 5,000 cps, most preferably from about 500 to 3,000 cps. For the purposes of this invention, the viscosity is ideo with a Broo field viscometer using an RV # 5 spindle at 50 p.
PREPARATION AND USE OF THE COMPOSITION the non-aqueous liquid detergent compositions herein can be prepared by combining the essential and optional components thereof in which < Iu? er convenient order and mixing, v.gr,., stirring, the resulting combination of components to form the stable compositions «Je phase of the present. In a typical process for preparing said compositions, essential components and certain preferred optional components will be combined in a particular order and under certain conditions. In the first step of said typical preparation process, a mixture of the surfactant of the alkylbenzene ammonium fonate and the two essential components of the non-aqueous diluent is formed by heating a combination of these materials to an emperature of about 30 ° C to 100 ° C. . In a second procedure step, the heated mixture formed as described above is maintained under shear agitation at a temperature of about 40 ° C to 100 ° C for a period of about 2 minutes to 20 hours. Optionally, you can apply vacuum to the mix at this point. This second process step serves to completely dissolve the ammonium surfactant in the non-aqueous liquid phase. In a third process step, this combination of phase 1 and 2 materials is cooled to a temperature of from about 0 ° C to 35 ° C. This cooling step serves to form a Luuide base which contains surfactant and surfactant in which the particulate material of the detergent compositions herein can be added and dispersed. The particulate material is added in a fourth process step by combining the particulate material with the liquid base which is maintained under shear agitation conditions. When adding particulate additives, the particulate material he prefers the observation of a certain order of addition. For example, while stirring the shear stress is maintained, essentially all the optional surfactants may be added in the form of solid particles in the form of particles ranging in size from about 0.2 to about 1,000 microns. After the addition of any optional surfactant particles, the particles of almost all of an organic builder can be added, eg, citrate and / or fatty acid and / or a source of alkalinity, v. carbonate, sodium carbonate, continuing with the maintenance of this mixture of components of the composition under agitation. * Other optional ingredients can be added in solid form to the composition at this point. The agitation of the mixture is continued and if necessary it can be increased at that point to form a uniform dispersion of solid phase particles. 4 l insolubles within «phase l« «| u? da. After a couple or all the solid materials have been added to this stirred mixture, the parts of the highly preferred peroxygen bleach agent can be added to the composition, again while the mixture is kept under shear agitation. Adding the peroxygen agent agent material at the end or after all or most of < As the components and especially after the particles of the alkalinity source have been added, the desirable stability benefits of the peroxygen bleach can be achieved. If "enzyme" pellets are incorporated, they are preferably added to the non-aqueous LiquLda matrix at the end. As a final step, after the addition of all the particulate material, stirring of the mixture is continued for a sufficient period of time to form compositions having the characteristics of viscosity and phase stability. required. Frequently, this will include agitation for a period of from about 1 to 30 minutes. In one variant of the process for preparing the composition described above, one or more of the solid components may be added to the stirred mixture as a suspension of pre-segregated particles with a lower portion of one or more of the liquid components. In this way, a premix can be formed separately from a small fraction of the alkoxy alcohol and / or the non-aqueous low polarity solvent with particles of the organic detergent-making material or the particles of the alkalinity source. inorganic and / or the particles of a bleach activator and added as a suspension to the stirred mixture of the components of the composition. The addition of said suspension pre-ezclas must precede the addition of the bleaching agent "peroxygen" or "enzyme particles" which may be part of an analogous pre-mix suspension. In the compositions of this invention, prepared as described above, they can be used to form aqueous wash solutions < * That they will be used in the washing and bleaching of fabrics. Generally, an effective amount of said compositions is added to the water, preferably in a conventional automatic fabric washing machine, to form said aqueous washing / bleaching solutions. The aqueous wash / bleach solution formed in this manner is then placed in contact, preferably under agitation, with the fabrics "to be washed and bleached therewith. An effective amount of the liquid detergent compositions herein added to water to form aqueous wash / bleach solutions, may comprise sufficient amounts to form about 500 to 7,000 pprn of the composition in aqueous solution. Most preferably, from about 800 to 3,000 pprn of the detergent compositions herein will be provided in the aqueous wash / bleach solution.
EXAMPLE The following example illustrates the compositions of the present invention, but is not necessarily designed to limit or otherwise "open the scope of the invention" to the present invention. An Intuido and non-aqueous washing detergent is prepared, which contains bleach having the cornposi cíoneís established in Table T.
Table I Component% by weight Liquid phase Alkylbenzene fonate linear of Na of C12 (LAS) 27.3 Ethoxylated alcohol of C12-1-, EO-5 10.6 Hexylene glycol 27.3 Perfume 0.4 Solids Protease Enzyme 0.4 Na3 citrate, anhydrous 4.3 Sodium perborate 3.4 Nonanoyloxybenzene sodium fonate (NOBS) 8.0 Carbonate «Je sodium 13.9 Acid dieti ltpami npent aaeeti co (J) TPA) 0.9 Brightener 0.4 S u p p re ss ss 0.1 Minor components 0.4 100% This composition is prepared by mixing LAS, hexylene glycol and alcohol ethoxylate with each other at 54 ° C during 1/2 hour This mixture is cooled "Jespues to 29 ° C after which the remaining components are added. The resulting composition is then stirred at 29 ° C for another 1/2 hour. The resulting composition is a heavy-duty, anhydrous and stable liquid washing detergent that provides excellent stain and dirt removal performance when used in normal washing operations.

Claims (9)

NOVELTY OF THE INVENTION CLAIMS
1. - A liquid and non-aqueous heavy-duty detergent composition in the form of a suspension of substantially insoluble particulate solid material dispersed through a liquid phase containing a surfactant and structured agent, said composition being characterized by ornaments because it comprises: ) of about 35% to 99% by weight of the composition of a nonaqueous liquid phase which comprises: i) from about 30% to 65% by weight of said nonaqueous liquid phase of a selected ammonium surfactant selected from the alkaline metal salts of the alkyl benzenesulonic acid of Cio-Ciß; V u) from about 35% to 70% by weight of said non-aqueous JK'Uida phase of a nonaqueous liquid diluent comprising a) alkoxy alcohol sides of the formula R1 (0Cffl H2m) n OH wherein R1 is a group Cs-Ciß alkyl, rn is from 2 to 4 and n is from about 2 to 12; and b) an organic solvent of low polarity and non-aqueous in a weight ratio of alcohol alkoxy to organic solvent of from about 50: 1 to 1:50; and B) from about 1% to 65% by weight of the composition of a particulate material ranging in size from about 0.1 to 1,500 microns, which is substantially more soluble in said non-aqueous liquid phase and which is selected from agents peroxygen bleach, bleach activators, LVOS auxiliary ammonia surfactants, organic mineral enhancers, morgam alkalinity sources and combinations of such materials.
2. A composition according to claim 1, wherein (A) the alkyl group of said alkylbenzene sulphonic acid is linear and contains from about 11 to 14 carbon atoms; (B) said alcohol alkoxylation component comprises ethoxylated materials < They contain from about 8 to 15 carbon atoms and they have from about 3 to 10 portions of ethylene oxide per * rnolecuLa; (C) said low polarity and non-aqueous organic solvent is selected from mono-alkyl esters of C2-Ce of mono-, di-, tri- or tetra-alkylene glycol of C2-C3; and 11) noncalcinal alkylene glycos containing from about 4 to 8 carbon atoms; and (D) said particulate material comprises per-oxygen bleach agents selected from percarboxylic acids and salts thereof and perborates and alkaline metal percarbones.
3. A composition according to claim 2, wherein (A) said ammonium surfactant agent aL-alkyl benzene sulphide comprises from about 15% to 60% by weight of the composition; (B) said non-aqueous liquid diluent comprises from about 15% to 70% by weight of the composition and has an alcohol ethoxylate to organic solvent ratio of from about 3: 1 to 1: 3; and (C) said particulate material comprises from about 5% to 50% by weight of the composition.
4. A composition according to claim 3, wherein (A) said bleaching agent is selected from perborates and percarbonates of alkali metal and comprises from about 1% to 30% by weight. weight of the composition; (B) said particulate material also comprises from about 0.5% to 20% by weight of the particulate composition of a bleach activator which can be recycled with said peroxygen bleach agent to form an? Er * ox? Ac? do.
5. A composition according to claim 4, which also contains about 1% to 20% by weight of the composition of an additional non-tonic surfactant comprising polymers of ethylene oxide block-propylene oxide.
6. A composition according to claim 4, wherein said particulate material also comprises from about 2% to 20% by weight of the composition of a detergent. The organic detergency selected from citrates, succinates, rnalonates, -box irnethylsuccinates, carboxylates, polycarboxylates, alkali metal polyacetyl carboxylates and fatty acid soaps.
7. A composition according to claim 6, wherein said organic detergency enhancer is sodium citrate. 40 p.- A composition "conforrn? da" J with claim 4, in the said particulate material also comprises "about 1% to 25% by weight of the composition of a selected alkalinity source" le carbonates , bicarbonates, borates, silicates and rnetasi Water-soluble alkali metal licates. 9. A composition according to claim 8, wherein "said source of alkalinity is a so-called cation. 10. A composition according to claim 4, containing on-line adLC of about 0.1% to 4% by weight of the composition of a chelating agent selected "Je arninocarbox Ltos, phosphonates, to innophostes, substituted aromatic chelating agents. pol i func onals and combinations of these agents quela adores. 11. A composition according to claim 10, wherein said chelating agent is selected from ac dietetic acid, nonpentaacetic acid, acid, ethylenitrile, dipicollic acid, and hydroxyethyldiphosphomatic acid and the salts of these chelating agents. 12. A composition according to claim 4, which additionally contains approximately "0.001% to 5% by weight of the composition of enzyme pellets wherein said pellets range in size from approximately LOO to 1,000 microns, and wherein said enzyme is selected from proteases, even lasas, cel or lasas and llpasas. 13. A composition according to claim 4, which contains additional (A) from about 0.1% to 4% by weight of the composition of thickener, viscosity control and / or dispersant selected from polymers based on acrylic acid, and has a molecular weight ranging from about 2,000 to 10,000; and / or (B) from about 0.0001% to 2% by weight of a polish *, suds suppressor, silicone oil, bleach catalyst, colorant and / or compatible perfume. 14. A liquid and non-aqueous heavy-duty detergent composition in the form of a slurry of peroxygen bleaching agent material substantially substantially soluble and solid dispersed through a liquid phase containing surfactant and structured agent having a viscosity of from about 300 to 5,000 cps, which composition is further characterized because it comprises: (A) from about 15% to 60% "of the composition of a linear alkyl benzene sulfate surfactant of Cn-C? alkaline; (B) from about 15% to 70% by weight of the composition of a non-aqueous liquid diluent comprising: i) an alcohol ethoxylate component comprising C 10 -C 14 alcohols containing from about 3 to 10 moles of oxide ethylene; and li) a nonaqueous organic solvent selected from diethylene glycol, rnononobutyl ether, monobuterol ether of dipropylengliol and hexyglial; in a ratio of the weight of ethoxylated alcohol to organic solvent of Jesde approximately 3: 1 to 1: 3; and (C) Approximately 1% to 20% by weight of the particulate composition of peroxygen bleach agent selected from perborates and percarbonates. Sodium and potassium, said particles ranging in size from about 5 to 200 microns. . 15. A composition according to claim cation 14, wherein said composition further comprises about 1% to 10% by weight of the bleach activator particle composition which can react with said bleaching agent. peroxygen to form a peroxyacid. 16. A composition according to claim 15, which additionally contains from about 4% to 10% by weight of the composition of an organic detergent selected from ci treats, succinates, allonates, carboxymethyl succemates, carboxylates, polycarboxylates, polyacetycarboxy alkali metal cans and fatty acid soaps. 17. A composition according to claim 16, which additionally contains from about 2% to 15% by weight of a source of selected alkali metal carbonates, bicarbonates, borates, silicates and metasilicates soluble in water. 1
8. A detergent composition "He weighs" the liquid "contains both bleach and non-aqueous agent comprising: (A) from about 20% to 40% by weight of the composition of an ammonium surfactant of alq? I Lbencens? Linear Sodium - Cia; (B) from about 5% to 25% by weight of the co-position of an alcohol ethoxylate of CIO-CIA, 1-3 EO; (C) "From about 10% to 30% by weight of the composition of hexylene glycol or nonobutyl ether of dipropyllelic acid; (D) of apr * ox? Rna «larnent or 1% to 20% by weight of the particulate composition of a peroxygen bleach agent selected from perborates and percarbonates of sodium and potassium; (E) from about L% to 10% of the particle composition of a bleach activator * selected from the following: nonanoyloxybenzene fonate, 6-alkaline do-cayro-lox and benzene sulfonate of Cs -Cio and tetraace i letilendia ina; and (F) from about 2% to 15% by weight of the composition of alkaline metal carbonate particles; and wherein said composition is in the form of suspension of particulate material comprising said particles dispersed through said liquid detergent composition, said particulate material varying in size from about 0.1% to 1,500 microns. 1
9. A composition according to claim 18, having from about 50% to 95% by weight of the composition of a liquid phase and from about 5% to 50% by weight of the composition of a solid particulate phase. 20.- A composition in accordance with 59Claim 19, which has a viscosity of from about 500 to 3,000 cps.
MXPA/A/1997/010504A 1995-06-20 1997-12-19 Compositions detergents liquid, non-aqueous, containing particles, that include a surgical agent of alquilbencensulfon MXPA97010504A (en)

Applications Claiming Priority (3)

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US34595P 1995-06-20 1995-06-20
US000345 1995-06-20
PCT/US1996/007814 WO1997000938A1 (en) 1995-06-20 1996-05-28 Nonaqueous, particulate-containing liquid detergent compositions with alkyl benzene sulfonate surfactant

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MX9710504A MX9710504A (en) 1998-03-29
MXPA97010504A true MXPA97010504A (en) 1998-10-15

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